Cas 1579268-79-3,N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

1579268-79-3

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Basic information

Product Name: N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide
Synonyms: N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide
CAS NO:1579268-79-3
Molecular Formula:
Molecular Weight: 632.802
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(1579268-79-3)
EPA Substance Registry System: N-(3-hydroxy-3-(5-methyl-1-tosyl-1H-indol-2-yl)propyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(1579268-79-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1579268-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1579268-79-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,2,6 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1579268-79:
(9*1)+(8*5)+(7*7)+(6*9)+(5*2)+(4*6)+(3*8)+(2*7)+(1*9)=233
233 % 10 = 3
So 1579268-79-3 is a valid CAS Registry Number.

1579268-79-3Upstream product

1579268-79-3Downstream Products

1579269-03-6 5-(4-methoxyphenyl)-9-methyl-2,6-ditosyl-1,2,3,4,5,6-hexahydroazepino[4,3-b]indole

1579268-79-3Relevant academic research and scientific papers

Synthesis of fused-tricyclic indole derivatives through an acid-promoted skeletal rearrangement

Yokosaka, Takuya,Kanehira, Tomoya,Nakayama, Hiroki,Nemoto, Tetsuhiro,Hamada, Yasumasa

, p. 2151 - 2160 (2014)

We developed a novel method for synthesizing fused-tricyclic indole derivatives with a 3-aminomethyl indole motif through a reaction cascade involving ipso-Friedel-Crafts alkylation of phenols, rearomatization of the spirocyclohexadienone unit, and iso-Pictet-Spengler reaction. Using TFA as an acid promoter, six-, seven-, and eight-membered ring-fused indoles were obtained in 31-99% yield.

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